August 2019 FDA Recall Drug by American Health Packaging
D-1821-2019 - Failed Dissolution Specifications

This Class II drug recall was voluntarily initiated by American Health Packaging on August 9, 2019 for the product Drug. The FDA reported the reason for recall as failed dissolution specifications. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1821-2019

Reason for Recall
Failed Dissolution Specifications
Initiated
08-09-2019
Reported
08-21-2019
Quantity
457 cartons

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
American Health Packaging
Carbamazepine, Extended-Release Tablets, USP, 400 mg, 30 Tablets (3 blister cards x 10 unit doses), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-562-21; NDC Unit Dose: 68084-562-11

Batch or Lot Expiration Information

Lot# Lot 181677, exp 11/30/2020